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PagerDuty, Inc.

15.91

+0.24001.53%

盘后：15.910.00000.00%17:17 EDT

成交量：126.84万

成交额：2,000.21万

市值：14.49亿

市盈率：-26.88

高：16.00

开：15.77

低：15.61

收：15.67

数据加载中...

总览公司新闻资讯公告

阿斯利康PD-L1单抗一项III期研究成功

从PD-1跟随到多款ADC领先，乐普生物-B（02157）迎价值重估？

【加科思-B(01167.HK)：SHP2抑制剂SITNEPROTAFIB联用研究数据发表于学术期刊】加科思-B(01167.HK)发布公告，公司自主研发的SHP2抑制剂sitneprotafib (JAB-3312)相关研究见刊Clinical Cancer Research(《临床肿瘤研究》)。文章公布了SHP2抑制剂与PD-1抗体以及靶向RTK/RAS/MAPK通路的联合疗法中的临床前体内外数据和对联合疗法有回应的代表性患者病例。

百济神州一季度亏损大幅收窄国内BTK抑制剂销售加速、PD-1销售减速

每日经济新闻

基石药业(02616)重磅发布CS2009(PD-1/VEGF/CTLA-4)最新临床前研究结果

港股异动 | 三生制药(01530)再涨超9% 抗VEGF/PD-1双特异性抗体707被纳入突破性治疗品种

康方生物依沃西获批用于PD-L1阳性肺癌治疗

【康方生物(09926.HK)：依达方®(依沃西，PD-1/VEGF)第二个适应症上市申请获得NMPA批准用于一线治疗PD-L1阳性NSCLC】康方生物(09926.HK)发布公告，由公司自主研发的全球首创双特异性抗体依达方®(依沃西，PD-1/VEGF)单药用于PD-L1阳性(TPS≥1%)的表皮生长因子受体(EGFR)基因突变阴性和间变性淋巴瘤激酶(ALK)阴性的局部晚期或转移性非小细胞肺癌(NSCLC)的一线治疗的新药上市申请(sNDA)，已获得中国国家药品监督管理局(NMPA)批准上市。这是依沃西获批上市的第二个适应症，让中国患者“率先用上全球最优治疗方案”成为现实。

康方生物(09926.HK)：依达方®(依沃西，PD-1/VEGF)第二个适应症上市申请获得NMPA批准，用于一线治疗PD-L1阳性NSCLC

【康方生物(09926.HK)安尼可®（派安普利，PD -1）获美国食品药品监督管理局批准两项适应症用于治疗晚期鼻咽癌】康方生物(09926.HK)发布公告，安尼可®(派安普利，PD-1)已获得美国食品药品监督管理局(FDA)批准上市，用于治疗复发或转移性鼻咽癌的一线治疗和以铂类为基础的至少一线化疗治疗失败后治疗的2项适应症。派安普利由公司自主研发并由正大天晴康方负责后续开发和商业化，也是公司第一个获得美国FDA批准上市的自主研发创新生物药。

康方生物(09926)安尼可®（派安普利，PD -1）获美国食品药品监督管理局批准两项适应症用于治疗晚期鼻咽癌

港股异动 | 信达生物(01801)涨超5% IBI363（PD-1/IL-2α-bias）等多款管线将亮相2025 ASCO

港股异动 | 基石药业-B(02616)最高涨超7% 三抗CS2009（PD-1/VEGF/CTLA-4）即将在AACR更新更多数据

荣获七项ASCO口头报告：信达生物IBI363（PD-1/IL-2α-bias）领衔多款管线亮相美国临床肿瘤学会2025年大会

Pagerduty, Inc.盘中异动早盘股价大涨5.08%

又一次“头对头”胜出！康方生物双抗药物疗效“击败”百济神州PD-1

康方生物在一项临床三期试验中赢了百济神州的PD-1抗体联合疗法

每日经济新闻

港股异动 | 康方生物(09926)涨超13%创历史新高康方PD-1/VEGF双抗首次战胜PD-1+化疗

百时美施贵宝（BMY.US）PD-1抑制剂在中国获批新适应症

智通财经网

港股异动 | 三生制药(01530)涨超3% 抗VEGF/PD-1双特异性抗体获国家药监局突破性疗法认定

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Research(《临床肿瘤研究》)。文章公布了SHP2抑制剂与PD-1抗体以及靶向RTK/RAS/MAPK通路的联合疗法中的临床前体内外数据和对联合疗法有回应的代表性患者病例。","market":"hk","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://24h.jrj.com.cn/2025/05/09064650243257.shtml","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":"jinrongjie_stock","symbols":["PD","BK1574","BK4023","LU1169590202.USD","01167","LU1169589451.USD","BK1161"],"gpt_icon":0},{"id":"2533932462","title":"百济神州一季度亏损大幅收窄 国内BTK抑制剂销售加速、PD-1销售减速","url":"https://stock-news.laohu8.com/highlight/detail?id=2533932462","media":"每日经济新闻","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2533932462?lang=zh_cn&edition=fundamental","pubTime":"2025-05-07 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抗VEGF/PD-1双特异性抗体707被纳入突破性治疗品种","url":"https://stock-news.laohu8.com/highlight/detail?id=2532724863","media":"智通财经","labels":["productRelease","movement"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2532724863?lang=zh_cn&edition=fundamental","pubTime":"2025-05-02 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09:32","pubTimestamp":1745803955,"startTime":"0","endTime":"0","summary":"4月27日，康方生物（09926）发布公告，宣布其自主研发的双特异性抗体依达方?（依沃西，PD-1/VEGF）获得中国国家药品监督管理局（NMPA）批准，用于一线治疗PD-L1阳性非小细胞肺癌（NSCLC）。这是依沃西获得的第二个适应症，标志着中国患者能够率先使用全球最优治疗方案。","market":"hk","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"http://finance.eastmoney.com/a/202504283390722024.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":"stock_eastmoney","symbols":["LU2488822045.USD","09926","LU1169589451.USD","BK1574","IE00B5MMRT66.SGD","LU0348783233.USD","IE00B543WZ88.USD","BK1161","BK4023","LU1720050803.USD","LU0348784397.USD","LU1169590202.USD","LU1794554557.SGD","PD","IE00BPRC5H50.USD","LU0417516571.SGD"],"gpt_icon":0},{"id":"2530343711","title":"【康方生物(09926.HK)：依达方®(依沃西，PD-1/VEGF)第二个适应症上市申请获得NMPA批准 用于一线治疗PD-L1阳性NSCLC】康方生物(09926.HK)发布公告，由公司自主研发的全球首创双特异性抗体依达方®(依沃西，PD-1/VEGF)单药用于PD-L1阳性(TPS≥1%)的表皮生长因子受体(EGFR)基因突变阴性和间变性淋巴瘤激酶(ALK)阴性的局部晚期或转移性非小细胞肺癌(NSCLC)的一线治疗的新药上市申请(sNDA)，已获得中国国家药品监督管理局(NMPA)批准上市。这是依沃西获批上市的第二个适应症，让中国患者“率先用上全球最优治疗方案”成为现实。","url":"https://stock-news.laohu8.com/highlight/detail?id=2530343711","media":"金融界","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2530343711?lang=zh_cn&edition=fundamental","pubTime":"2025-04-27 20:01","pubTimestamp":1745755264,"startTime":"0","endTime":"0","summary":"康方生物(09926.HK)发布公告，由公司自主研发的全球首创双特异性抗体依达方®(依沃西，PD-1/VEGF)单药用于PD-L1阳性(TPS≥1%)的表皮生长因子受体(EGFR)基因突变阴性和间变性淋巴瘤激酶(ALK)阴性的局部晚期或转移性非小细胞肺癌(NSCLC)的一线治疗的新药上市申请(sNDA)，已获得中国国家药品监督管理局(NMPA)批准上市。这是依沃西获批上市的第二个适应症，让中国患者“率先用上全球最优治疗方案”成为现实。","market":"hk","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://24h.jrj.com.cn/2025/04/27200149930796.shtml","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"2","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":"jinrongjie_stock","symbols":["BK4585","IE00BPRC5H50.USD","LU1794554557.SGD","LU0348784397.USD","BK1161","BK4008","09926","IE00B543WZ88.USD","IE00B5MMRT66.SGD","LU1169589451.USD","LU0348783233.USD","BK4500","LU1169590202.USD","BK1574","BK4023","LU2488822045.USD","PD","ALK","LU1720050803.USD","LU0417516571.SGD","BK4588"],"gpt_icon":0},{"id":"2530379034","title":"康方生物(09926.HK)：依达方®(依沃西，PD-1/VEGF)第二个适应症上市申请获得NMPA批准，用于一线治疗PD-L1阳性NSCLC","url":"https://stock-news.laohu8.com/highlight/detail?id=2530379034","media":"格隆汇","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2530379034?lang=zh_cn&edition=fundamental","pubTime":"2025-04-27 19:58","pubTimestamp":1745755137,"startTime":"0","endTime":"0","summary":"格隆汇4月27日丨康方生物宣布，由公司自主研发的全球首创双特异性抗体依达方单药用于PD-L1阳性的表皮生长因子受体基因突变阴性和间变性淋巴瘤激酶阴性的局部晚期或转移性非小细胞肺癌的一线治疗的新药上市申请，已获得中国国家药品监督管理局批准上市。这是依沃西获批上市的第二个适应症，让中国患者‘‘率先用上全球最优治疗方案’’成为现实。依沃西是全球首个在头对头帕博利珠单抗的III期临床研究中获得显著阳性结果的药物。","market":"sh","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://finance.jrj.com.cn/2025/04/27195849930778.shtml","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":"jinrongjie_stock","symbols":["BK4023","IE00B543WZ88.USD","PD","09926","BK1574","IE00B5MMRT66.SGD","LU1169589451.USD","LU1169590202.USD","LU2488822045.USD","LU0348784397.USD","LU0417516571.SGD","LU1794554557.SGD","LU0348783233.USD","IE00BPRC5H50.USD","LU1720050803.USD","BK1161"],"gpt_icon":1},{"id":"2530916455","title":"【康方生物(09926.HK)安尼可®（派安普利，PD -1）获美国食品药品监督管理局批准 两项适应症用于治疗晚期鼻咽癌】康方生物(09926.HK)发布公告，安尼可®(派安普利，PD-1)已获得美国食品药品监督管理局(FDA)批准上市，用于治疗复发或转移性鼻咽癌的一线治疗和以铂类为基础的至少一线化疗治疗失败后治疗的2项适应症。派安普利由公司自主研发并由正大天晴康方负责后续开发和商业化，也是公司第一个获得美国FDA批准上市的自主研发创新生物药。","url":"https://stock-news.laohu8.com/highlight/detail?id=2530916455","media":"金融界","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2530916455?lang=zh_cn&edition=fundamental","pubTime":"2025-04-25 08:18","pubTimestamp":1745540328,"startTime":"0","endTime":"0","summary":"康方生物(09926.HK)发布公告，安尼可®(派安普利，PD-1)已获得美国食品药品监督管理局(FDA)批准上市，用于治疗复发或转移性鼻咽癌的一线治疗和以铂类为基础的至少一线化疗治疗失败后治疗的2项适应症。派安普利由公司自主研发并由正大天晴康方负责后续开发和商业化，也是公司第一个获得美国FDA批准上市的自主研发创新生物药。","market":"sh","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://24h.jrj.com.cn/2025/04/25081849860793.shtml","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"jinrongjie_stock","symbols":["IE00BPRC5H50.USD","09926","IE00B5MMRT66.SGD","LU1169590202.USD","LU0348783233.USD","IE00B543WZ88.USD","LU0417516571.SGD","LU1169589451.USD","LU1720050803.USD","LU2488822045.USD","PD","BK1161","159839","BK4023","LU0348784397.USD","BK1574","LU1794554557.SGD"],"gpt_icon":0},{"id":"2530191575","title":"康方生物(09926)安尼可®（派安普利，PD -1）获美国食品药品监督管理局批准 两项适应症用于治疗晚期鼻咽癌","url":"https://stock-news.laohu8.com/highlight/detail?id=2530191575","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2530191575?lang=zh_cn&edition=fundamental","pubTime":"2025-04-25 08:13","pubTimestamp":1745539980,"startTime":"0","endTime":"0","summary":"智通财经APP讯，康方生物 发布公告，安尼可已获得美国食品药品监督管理局批准上市，用于治疗复发或转移性鼻咽癌的一线治疗和以铂类为基础的至少一线化疗治疗失败后治疗的2项适应症。派安普利由公司自主研发并由正大天晴康方负责后续开发和商业化，也是公司第一个获得美国FDA批准上市的自主研发创新生物药。派安普利本次在美国获批上市，为全球的晚期鼻咽癌患者提供了免疫治疗新选择。","market":"hk","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"http://www.zhitongcaijing.com/content/detail/1284598.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"2","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":"stock_zhitongcaijing","symbols":["BK1574","LU0417516571.SGD","LU0348783233.USD","09926","LU0348784397.USD","LU1720050803.USD","LU2488822045.USD","IE00B543WZ88.USD","IE00B5MMRT66.SGD","LU1794554557.SGD","LU1169590202.USD","PD","IE00BPRC5H50.USD","BK1161","BK4023","LU1169589451.USD"],"gpt_icon":0},{"id":"2529640246","title":"港股异动 | 信达生物(01801)涨超5% IBI363（PD-1/IL-2α-bias）等多款管线将亮相2025 ASCO","url":"https://stock-news.laohu8.com/highlight/detail?id=2529640246","media":"智通财经","labels":["conferences","movement"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2529640246?lang=zh_cn&edition=fundamental","pubTime":"2025-04-24 14:37","pubTimestamp":1745476662,"startTime":"0","endTime":"0","summary":"智通财经APP获悉，信达生物涨超5%，截至发稿，涨5.05%，报54.05港元，成交额15.91亿港元。消息面上，4月24日，信达生物宣布将在美国临床肿瘤学会年会上展示肿瘤创新管线的一系列临床数据。其中，IBI363在黑色素瘤、肠癌、非小细胞肺癌的临床研究，以及 IBI343在胰腺癌研究方面均有口头报告。本届 ASCO 年会将于当地时间2025年5月30日-6月3日在美国芝加哥举办。","market":"hk","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"http://www.zhitongcaijing.com/content/detail/1283860.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"conferences,movement","news_rank":0,"length":0,"strategy_id":0,"source":"stock_zhitongcaijing","symbols":["LU2328871848.SGD","LU1169590202.USD","BK1589","LU1969619763.USD","PD","BK1161","LU2488822045.USD","BK1583","BK4023","01801","LU1169589451.USD"],"gpt_icon":0},{"id":"2529617317","title":"港股异动 | 基石药业-B(02616)最高涨超7% 三抗CS2009（PD-1/VEGF/CTLA-4）即将在AACR更新更多数据","url":"https://stock-news.laohu8.com/highlight/detail?id=2529617317","media":"智通财经","labels":["dataReport","movement"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2529617317?lang=zh_cn&edition=fundamental","pubTime":"2025-04-24 11:35","pubTimestamp":1745465743,"startTime":"0","endTime":"0","summary":"智通财经APP获悉，基石药业-B早盘最高涨超7%，截至发稿，涨2.41%，报2.97港元，成交额1672.07万港元。基石药业5款自主研发创新药物的最新临床前研究成果将同时亮相这一国际顶级学术舞台，包括三抗CS2009、双抗CS2011及出自公司自有抗体偶联药物平台的三款创新ADC分子CS5006、CS5007与CS5005。其中90%用于与集团“管线2.0”中的资产，尤其是CS5001，以及CS2009有关的进一步研发；余下净额于适当时用于其他一般公司用途。","market":"hk","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"http://www.zhitongcaijing.com/content/detail/1283807.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"dataReport,movement","news_rank":0,"length":0,"strategy_id":0,"source":"stock_zhitongcaijing","symbols":["BK1161","02616","BK4023","PD","BK1574","LU1169590202.USD","LU1169589451.USD"],"gpt_icon":0},{"id":"2529693739","title":"荣获七项ASCO口头报告：信达生物IBI363（PD-1/IL-2α-bias）领衔多款管线亮相美国临床肿瘤学会2025年大会","url":"https://stock-news.laohu8.com/highlight/detail?id=2529693739","media":"美通社","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2529693739?lang=zh_cn&edition=fundamental","pubTime":"2025-04-24 07:00","pubTimestamp":1745449200,"startTime":"0","endTime":"0","summary":"本届 ASCO 年会将于当地时间2025年5月30日-6月3日在美国芝加哥举办。信达生物制药集团高级副总裁周辉博士表示：\"很高兴在本次ASCO大会上，IBI363开发的第一批三大适应症黑色素瘤、肠癌、非小细胞肺癌的临床研究均被接收为口头报告，代表了下一代PD-1双抗肿瘤免疫疗法引起了全球的广泛关注。同时IBI343胰腺癌研究继去年12月ESMO Asia口头报告之后，再次以口头报告登上ASCO舞台。","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://wwwold.prnasia.com/story/archive/4671176_ZH71176_1","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"dataReport","news_rank":0,"length":0,"strategy_id":0,"source":"prnasia","symbols":["LU2328871848.SGD","BK4139","IVBIY","01801","LU1169589451.USD","BK1589","LU1169590202.USD","LU2488822045.USD","BK4023","BK1583","LU1969619763.USD","BK1161","PD"],"gpt_icon":1},{"id":"2529687522","title":"Pagerduty, Inc.盘中异动 早盘股价大涨5.08%","url":"https://stock-news.laohu8.com/highlight/detail?id=2529687522","media":"市场透视","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2529687522?lang=zh_cn&edition=fundamental","pubTime":"2025-04-23 21:40","pubTimestamp":1745415624,"startTime":"0","endTime":"0","summary":"北京时间2025年04月23日21时40分，Pagerduty, Inc.股票出现异动，股价大幅上涨5.08%。Pagerduty, Inc.股票所在的软件服务行业中，整体涨幅为3.35%。其相关个股中，Pegasystems Inc.、Apptech Payments Corp C/Wts 04/01/2027 、Triller Group Inc C/Wts 15/03/2027 涨幅较大，Femto Technologies Inc.、Microalgo, Inc.、Oblong Inc.较为活跃，换手率分别为15.88%、12.57%、11.91%，振幅较大的相关个股有Triller Group Inc C/Wts 15/03/2027 、Femto Technologies Inc.、百家云，振幅分别为18.07%、15.28%、13.36%。Pagerduty, Inc.公司简介：PagerDuty 是一个数字运营管理平台，可为现代数字业务管理紧急和任务关键型工作。","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tencent","url":"http://gu.qq.com/resources/shy/news/detail-v2/index.html#/?id=nesSN20250423214025aa2c7890&s=b","rn_cache_url":null,"customStyle":"body{padding-top:10px;}#news_title{font-weight:bold;#titleStyle#;}#news_description span{font-size:12px;#descriptionStyle#;}.footer-note{#statement#}","selectors":".mod-LoadTzbdNews, body","filters":".relate-stock, .hot-list, .recom-box, 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